Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)
Location

Chromosome 14:103712977 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5, Illumina_Human1M-duo

About this variant

This variant overlaps 22 transcripts, has 1532 individual genotypes and is mentioned in 2 citations.

Variation displays